Cockar Iram, Foskett Pierre, Strautnieks Sandra, Clinch Yasmin, Fustok Jana, Rahman Obydur, Sutton Harry, Mtegha Marumbo, Fessatou Smaragdi, Kontaki Elena, Papaevangelou Vassiliki, Deheragoda Maesha, Thompson Richard J, Grammatikopoulos Tassos
Paediatric Liver, GI & Nutrition Centre and MowatLabs.
Institute of Liver Studies, King's College Hospital, London.
J Pediatr Gastroenterol Nutr. 2020 Aug;71(2):184-188. doi: 10.1097/MPG.0000000000002740.
Mutations in Myosin 5B (MYO5B) are known to be associated with microvillous inclusion disease (MVID) a genetic cause of neonatal intractable diarrhoea. More recently, they have been reported in children with cholestasis but without typical gastrointestinal symptoms of MVID. We describe our series of children with cholestasis and mutations in MYO5B.
Clinical, laboratory, and histological data were collected from patients with cholestasis and pathogenic mutations in MYO5B, found by next generation sequencing (NGS) but with minimal gastrointestinal disease.
Six patients (3 boys) were identified. Median age at presentation was 19 months (range, 3-92). Presenting features were jaundice, pale stools, pruritus, and failure to thrive. Patients 5 and 6 had intractable diarrhoea until the age of 3 and 7 years, respectively, but currently are on full enteral diet with no intestinal symptoms. Median values for serum total bilirubin were 55 μmol/L (2-500), alanine aminotransferase 73I IU/L (32-114), γ-glutamyltransferase 7 IU/L (7-10), and serum bile acids 134 μmol/L (18-274). Three patients underwent 1 or more types of biliary diversion for symptom control. Median follow-up was 5 years (2-22). At most recent follow-up, they all reported pruritus while on antipruritics. Patient 1 had a liver transplant.
We identified 6 patients, with mutations in MYO5B, early-onset cholestasis and pruritus, with variable response to biliary diversion without typical MVID.
已知肌球蛋白5B(MYO5B)突变与微绒毛包涵体病(MVID)相关,MVID是新生儿顽固性腹泻的一个遗传病因。最近,有报道称在胆汁淤积但无MVID典型胃肠道症状的儿童中发现了这些突变。我们描述了我们收治的一系列患有胆汁淤积且MYO5B发生突变的儿童。
收集通过下一代测序(NGS)发现有MYO5B致病突变但胃肠道疾病轻微的胆汁淤积患者的临床、实验室和组织学数据。
共确定了6例患者(3名男孩)。就诊时的中位年龄为19个月(范围3 - 92个月)。主要表现为黄疸、浅色粪便、瘙痒和生长发育迟缓。患者5和患者6分别在3岁和7岁之前患有顽固性腹泻,但目前完全采用肠内饮食且无肠道症状。血清总胆红素的中位值为55μmol/L(2 - 500),丙氨酸氨基转移酶为73 IU/L(32 - 114),γ-谷氨酰转移酶为7 IU/L(7 - 10),血清胆汁酸为134μmol/L(18 - 274)。3例患者接受了1种或多种类型的胆汁转流术以控制症状。中位随访时间为5年(2 - 22年)。在最近一次随访时,他们在使用止痒药的情况下均报告有瘙痒症状。患者1进行了肝移植。
我们确定了6例MYO5B发生突变、早发性胆汁淤积和瘙痒的患者,他们对胆汁转流术反应不一,且无典型的MVID。